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1دورية أكاديمية
المؤلفون: De Wachter, Matthias, Schoonjans, An-Sofie, Weckhuysen, Sarah, Van Schil, Kristof, Löfgren, Ann, Meuwissen, Marije, Jansen, Anna, Ceulemans, Berten
المصدر: In European Journal of Paediatric Neurology January 2024 48:46-60
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2دورية أكاديمية
المؤلفون: Timmerman, Vincent, Löfgren, Ann, Le Guern, Eric, Liang, Ping, De Jonghe, Peter, Martin, Jean-Jacques, Verhalle, Damienne, Robberecht, Wim, Gouider, Riadh, Brice, Alexis, Van Broeckhoven, Christine
المصدر: Human Genetics. January 1996 97(1):26-34
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المؤلفون: Gert Van Goethem, Rik Vandenberghe, Löfgren Ann, Annelies Quaegebeur, Katrien Smets, Wim Van Paesschen, Wouter Janssen
المصدر: Acta neurologica Belgica
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Pediatrics, medicine.medical_specialty, Ataxia, Neurology, Adolescent, DNA Mutational Analysis, DNA-Directed DNA Polymerase, Status epilepticus, Young Adult, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Fluorodeoxyglucose F18, Humans, Medicine, Child, business.industry, Electroencephalography, General Medicine, medicine.disease, Magnetic Resonance Imaging, DNA Polymerase gamma, 030104 developmental biology, Migraine, Positron-Emission Tomography, Anesthesia, Mutation, Epilepsy syndromes, Female, Neurology (clinical), Human medicine, medicine.symptom, business, Occipital lobe, Polyneuropathy, 030217 neurology & neurosurgery
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المؤلفون: Löfgren, Ann
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_______261::0f26310eb41cbdd248bbd8b8398961c7
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-105145 -
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المؤلفون: Löfgren, Ann
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_______681::0f26310eb41cbdd248bbd8b8398961c7
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-105145 -
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المؤلفون: Kochañski, A., Timmerman, Vincent, Jêdrzejowska, H., Ryniewicz, B., Löfgren, Ann, De Vriendt, Els, Wouters, V., Van Broeckhoven, Christine, Latos-Bieleñska, A., Hausmanowa-Petrusewicz, I.
المصدر: Annals of the New York Academy of Sciences
مصطلحات موضوعية: Genetic Markers, Male, Pediatrics, medicine.medical_specialty, business.industry, General Neuroscience, Chromosome Mapping, Connexins, General Biochemistry, Genetics and Molecular Biology, Pedigree, History and Philosophy of Science, Charcot-Marie-Tooth Disease, Mutation screening, medicine, Humans, Female, Genetic Testing, Poland, business, Myelin P0 Protein, Myelin Proteins, Polymorphism, Restriction Fragment Length, Chromosomes, Human, Pair 17
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المؤلفون: Kurt, Bulent, Jaeken, Jaak, Van Hove, Johan, Löfgren, Ann, Van Goethem, Gert
المصدر: Archives of neurology
مصطلحات موضوعية: Human medicine
وصف الملف: pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2097::33ce4e0ea12bc8c94f04eb3459d1aef9
https://hdl.handle.net/10067/956430151162165141 -
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المؤلفون: Barisic, N., Claeys, Kristl G., Sirotković-Skerlev, M., Löfgren, Ann, Nelis, Eva, De Jonghe, Peter, Timmerman, Vincent
المصدر: Annals of human genetics
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Charcot-Marie-Tooth disease, Genetics, Clinico-Genetic confrontation, nervous system diseases
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المؤلفون: Claes, L., Ceulemans, Berten, Audenaert, Dominique, Smets, Katrien, Löfgren, Ann, Del-Favero, Jurgen, Ala-Mello, S., Basel-Vanagaite, L., Plecko, B., Raskin, S., Thiry, P., Wolf, N.I., Van Broeckhoven, Christine, De Jonghe, Peter
المصدر: Human mutation
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المؤلفون: Pou-Serradell, A., Monells, J., Téllez, M.J., Fossas, P., Löfgren, Ann, Meuleman, J., Timmerman, Vincent, De Jonghe, Peter, Ceuterick-de Groote, Chantal, Martin, Jean-Jacques
المصدر: Revue neurologique
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2097::1cf73c14a4606232762fdead9d61b60e
https://hdl.handle.net/10067/390530151162165141